A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660809



Internal ID9926914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24527795..24535101hg38UCSC Ensembl
Outerchr16:24527424..24535471hg38UCSC Ensembl
Innerchr16:24539116..24546422hg19UCSC Ensembl
Outerchr16:24538745..24546792hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg388048
hg198048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5600147, essv5643431, essv6462149, essv6239120, essv5597312, essv5467913, essv5894977, essv5618524, essv5715452, essv5833698, essv5594759, essv5410926, essv6057414, essv5771807
SamplesNA19701, NA19703, NA20294, NA20332, NA19920, NA20317, NA19901, NA20342, NA20127, NA19982, NA20296, NA19835, NA19818, NA20348
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660809
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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